6-HEPTEN-1-OL manufacturers
- 6-Hepten-1-ol
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- $2.20
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2026-07-02
- CAS:4117-10-6
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 50kg
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| | 6-HEPTEN-1-OL Basic information |
| | 6-HEPTEN-1-OL Chemical Properties |
| Melting point | 26°C (estimate) | | Boiling point | 113 °C / 69mmHg | | density | 0,85 g/cm3 | | refractive index | 1.4380 to 1.4420 | | pka | 15.19±0.10(Predicted) | | form | clear liquid | | color | Colorless to Almost colorless | | InChI | InChI=1S/C7H14O/c1-2-3-4-5-6-7-8/h2,8H,1,3-7H2 | | InChIKey | UFULDTPDHIRNGS-UHFFFAOYSA-N | | SMILES | C(O)CCCCC=C |
| Risk Statements | 10 | | Safety Statements | 16 | | RIDADR | 1987 | | HazardClass | 3 | | PackingGroup | III | | HS Code | 2905299090 |
| | 6-HEPTEN-1-OL Usage And Synthesis |
| Uses | 6-Hepten-1-ol has a floral and green odor and is commonly used as a flavoring agent in the food and beverage industry. In addition, it can be used as an intermediate in the synthesis of various organic compounds, including fragrances, pharmaceuticals, and agrochemicals. Its unique chemical properties make it an important ingredient in a variety of industrial processes, notably in the production of perfumes, air fresheners and cleaning agents. | | Industrial uses | 6-Hepten-1-ol is used as a flavoring agent in the food and beverage
industry. Its fruity and pear-like aroma makes it suitable for creating
or enhancing the taste of various fruit-flavored products, such as
beverages, confectionery, and ice cream. | | Synthesis | 4-Bromo-1-butanol (15.3g,0.1mol) was dissolved in 100ml of anhydrous tetrahydrofuran, anhydrous tetrahydrofuran solution of allylmagnesium chloride (0.25mol,250ml,1M) and lithium tetrachlorocopperate (10mmol,0.2mol/L,50ml) were added dropwise at 0, the reaction was continued for 15 hours, and then the reaction was stopped by addition of saturated ammonium chloride. After the reaction was continued for 15 hours, the reaction was aborted by adding appropriate amount of saturated ammonium chloride solution, the tetrahydrofuran was evaporated, and ethyl acetate was added to extract three times, the organic layer was dried with anhydrous sodium sulfate and the solvent was evaporated to obtain the crude product, and the decompression distillation yielded 6-hepten-1-ol (4) 9.8 g, with the yield of 86%. |
| | 6-HEPTEN-1-OL Preparation Products And Raw materials |
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